Canonical Allele Identifier: PA2829969160
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709802
ClinVar RCV Id: RCV002290144
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Arg400Leu
CA351074944
NM_021027.3:c.1199G>T